JPH0381185A - Coupling medium - Google Patents
Coupling mediumInfo
- Publication number
- JPH0381185A JPH0381185A JP1217819A JP21781989A JPH0381185A JP H0381185 A JPH0381185 A JP H0381185A JP 1217819 A JP1217819 A JP 1217819A JP 21781989 A JP21781989 A JP 21781989A JP H0381185 A JPH0381185 A JP H0381185A
- Authority
- JP
- Japan
- Prior art keywords
- base sheet
- thermoplastic resin
- resin layer
- medium
- color
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 230000008878 coupling Effects 0.000 title abstract 3
- 238000010168 coupling process Methods 0.000 title abstract 3
- 238000005859 coupling reaction Methods 0.000 title abstract 3
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 41
- 239000002243 precursor Substances 0.000 claims abstract description 9
- 238000003486 chemical etching Methods 0.000 claims description 2
- 239000003094 microcapsule Substances 0.000 abstract description 11
- 238000007788 roughening Methods 0.000 abstract 1
- 239000004576 sand Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 12
- 230000001070 adhesive effect Effects 0.000 description 11
- 239000000853 adhesive Substances 0.000 description 10
- 239000000123 paper Substances 0.000 description 10
- -1 postcards Substances 0.000 description 9
- 239000002985 plastic film Substances 0.000 description 8
- 229920006255 plastic film Polymers 0.000 description 8
- 239000004744 fabric Substances 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 239000003999 initiator Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000010008 shearing Methods 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 2
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000012965 benzophenone Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone Chemical class C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 description 2
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 238000012695 Interfacial polymerization Methods 0.000 description 1
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- ZKURGBYDCVNWKH-UHFFFAOYSA-N [3,7-bis(dimethylamino)phenothiazin-10-yl]-phenylmethanone Chemical compound C12=CC=C(N(C)C)C=C2SC2=CC(N(C)C)=CC=C2N1C(=O)C1=CC=CC=C1 ZKURGBYDCVNWKH-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical class C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Color Printing (AREA)
Abstract
Description
【発明の詳細な説明】
【産業上の利用分野]
本発明は、ベースシート上に少なくとも顕色剤層と、熱
可塑性樹脂層とを有し、普通紙、布地。Detailed Description of the Invention [Industrial Application Field] The present invention provides a base sheet having at least a color developer layer and a thermoplastic resin layer, plain paper or cloth.
プラスチックフィルム等に画像を形成することを可能に
する顕色媒体に関するものである[従来技術]
従来、光硬化性物質、光重合開始剤、染料前駆体を主内
包物とするマイクロカプセルと、マイクロカプセルの内
包物である染料前駆体と反応して呈色する物質いわゆる
顕色剤とが同一表面に塗布された感光感圧記録媒体が知
られている。また前記マイクカプセルと顕色剤とが別々
のシートに塗布されたものもある。(特開昭58−23
025号公報、特開昭58−88739号公報、特開昭
58−88740号公報等)。This relates to a color developing medium that makes it possible to form images on plastic films, etc. [Prior art] Conventionally, microcapsules mainly containing a photocurable substance, a photopolymerization initiator, and a dye precursor; A photosensitive pressure sensitive recording medium is known in which a substance that develops color by reacting with a dye precursor contained in a capsule, that is, a color developer, is coated on the same surface. There is also one in which the microphone capsule and the color developer are coated on separate sheets. (Unexamined Japanese Patent Publication No. 58-23
025, JP-A-58-88739, JP-A-58-88740, etc.).
この種の記録媒体は、光により光硬化性物質が硬化しマ
イクロカプセルが剛体となるので、通常表面を画像情報
に応じて露光し、露光によって硬化しなかったマイクロ
カプセルが破壊することで内部の染料前駆体が記録媒体
表面上、あるいは別のシートに塗布された顕色剤と反応
し、画像を形成する装置に用いられている。しかしなが
ら、この感光感圧記録媒体によれば、特殊加工された感
光感圧シートそのもの、あるいは前述の顕色剤層のみの
顕色シートに記録形成することは可能であるがこれと同
品質の画像をハガキ等普通用紙、布。In this type of recording medium, the photocurable substance is cured by light and the microcapsules become rigid, so the surface is usually exposed to light according to the image information, and the microcapsules that have not been hardened by exposure are destroyed and the internal parts are A dye precursor is used in a device that forms an image by reacting with a color developer coated on the surface of a recording medium or on another sheet. However, according to this photosensitive and pressure sensitive recording medium, it is possible to record and form images on the specially processed photosensitive and pressure sensitive sheet itself, or on the aforementioned color developer sheet with only a color developer layer, but it is possible to produce images of the same quality. Ordinary paper such as postcards, cloth.
プラスチックフィルム等、任意のものに画像を記録形成
できないという問題点があった。There was a problem that images could not be recorded on arbitrary materials such as plastic films.
そこで、ベースシート上に熱可塑性樹脂層を、またその
熱可塑性樹脂層上にさらに顕色剤層を有することを特徴
とする顕色媒体と、マイクロカプセルを担持する感光感
圧シートを用いて顕色媒体の顕色剤層上に画像を形成し
2、画像の形成された顕色剤層面と、普通紙、布等の被
画像形成体面とを合わせ、加熱し、ベースシートのみ剥
がし取る方法が考えられている。Therefore, a color developing medium characterized by having a thermoplastic resin layer on a base sheet and a color developer layer further on the thermoplastic resin layer, and a photosensitive pressure sensitive sheet supporting microcapsules were developed. There is a method in which an image is formed on the developer layer of a color medium, 2, the surface of the developer layer on which the image is formed is aligned with the surface of the object on which the image is formed, such as plain paper or cloth, heated, and only the base sheet is peeled off. It is considered.
[発明が解決しようとする課題]
しかしながら、従来の顕色媒体のベースシートは、ベー
スシート表面が比較的平滑度の高いポリエステルフィル
ム、ポリエチレンフィルム、ポリプロピレンフィルム等
を用いたため顕色剤層に、画像を形成するための圧力定
着時に熱可塑性樹脂がベースシートから剥がれてしまう
ことがしばしば起こった。[Problems to be Solved by the Invention] However, since the base sheet of the conventional color developing medium uses polyester film, polyethylene film, polypropylene film, etc., which have a relatively smooth surface, the color developer layer does not have the image quality. The thermoplastic resin often peeled off from the base sheet during pressure fixing to form the base sheet.
また、普通紙、布等の被画像形成体面に画像の形成され
た顕色媒体の顕色剤層を転写し、ベースシートを剥ぎ取
った後、ベースシートの表面状態がそのまま熱可塑性樹
脂の表面状態となり光沢のある状態となった。この光沢
のある状態ではキズ。In addition, after transferring the color developer layer of the color developer medium on which the image is formed onto the surface of the image-forming object such as plain paper or cloth and peeling off the base sheet, the surface condition of the base sheet remains unchanged on the surface of the thermoplastic resin. It became shiny and shiny. There are scratches in this shiny state.
また指紋等の汚れが目立ち、見栄えが悪く画質の低下と
なっていた。In addition, stains such as fingerprints were noticeable, resulting in poor appearance and deterioration in image quality.
本発明は、上述した問題点を解決するためになされたも
のであり、その第一の目的は簡単、迅速。The present invention was made to solve the above-mentioned problems, and its first purpose is to make it simple and quick.
確実に普通紙、プラスチックフィルム等に顕色剤画像を
一回の転写工程で形成できる顕色媒体のベースシートと
熱可塑性樹脂層との接着力を増大させ、圧力定着時に起
こる熱可塑性樹脂層のベースシートからの剥離を防ぐこ
とにある。また、第二の目的は、普通紙、プラスチック
フィルム等に顕色剤画像を転写した後、熱可塑性樹脂表
面をマット加工したようにすることで傷、汚れを目立た
なくし、見栄えをよくし、画像品質を向上させることに
ある。A developer image can be reliably formed on plain paper, plastic film, etc. in a single transfer process.It increases the adhesive strength between the base sheet of the developer medium and the thermoplastic resin layer, and prevents the formation of the thermoplastic resin layer that occurs during pressure fixing. The purpose is to prevent peeling from the base sheet. The second purpose is to transfer the color developer image to plain paper, plastic film, etc. and then apply a matte finish to the thermoplastic resin surface to make scratches and dirt less noticeable, improve the appearance, and improve the appearance of the image. The goal is to improve quality.
[課題を解決するための手段]
この目的を達成するために本発明の顕色媒体はベースシ
ート上に熱可塑性樹脂層、さらに熱可塑性樹脂層上に顕
色剤層を有する構造となっており、そのベースシートは
両面または片面が粗面となっている。[Means for Solving the Problems] In order to achieve this object, the color developing medium of the present invention has a structure in which a thermoplastic resin layer is provided on a base sheet, and a color developer layer is further provided on the thermoplastic resin layer. , the base sheet has a rough surface on both or one side.
[作用]
上記の構成を有する本発明の顕色媒体のベースシートは
粗面となったので、熱可塑性樹脂とベースシートの接着
力が増し、またベースシートを剥がし取った後、熱可塑
性樹脂が表面の荒れたベースシートで型押しされた形と
なり熱可塑性樹脂の表面がマット加工したようになる。[Function] Since the base sheet of the color developing medium of the present invention having the above structure has a rough surface, the adhesive force between the thermoplastic resin and the base sheet increases, and after the base sheet is peeled off, the thermoplastic resin The base sheet has a rough surface and is embossed, giving the thermoplastic resin a matte finish.
[実施例]
以下、本発明を具体化した一実施例を図面を参照して説
明する。[Example] Hereinafter, an example embodying the present invention will be described with reference to the drawings.
第1図は本発明の顕色媒体の断面図である。顕色媒体1
は表面が荒らされたベースシート2上に熱可塑性樹脂3
をまたさらに熱可塑性樹脂3上に顕色剤層4を有する。FIG. 1 is a sectional view of the color developing medium of the present invention. Color developing medium 1
is a thermoplastic resin 3 on a base sheet 2 with a roughened surface.
Furthermore, a color developer layer 4 is provided on the thermoplastic resin 3.
まず、第2図〜第4図に従って普通紙、プラスチックフ
ィルム、布等の被画像形成体面5に顕色剤画像を形成す
る方法を説明する。第3図は感光感圧媒体10に潜像を
形成する方法の説明図である。図示する様にまず光源3
0からの光を原稿20を介して照射すると原稿20の透
過部分20aに対応した感光感圧媒体10のマイクロカ
プセル11aのみが露光され、これによってその部分の
マイクロカプセルllaが硬化するのでその後第4図に
示す様に圧力ローラ40を用いて加圧すれば硬化してい
ないマイクロカプセルllbのみが破壊され、内部の染
料前駆物質が顕色剤4上に流出してその部分が発色し、
原稿20の画像の同一の逆像画像を形成する。この時本
発明の顕色媒体のベースシートがサンドブラスト加工さ
れているので、熱可塑性樹脂とベースシートとの接着が
強く圧力ローラ40を通しても剥がれることはない。First, a method for forming a color developer image on the surface 5 of an image-forming object such as plain paper, plastic film, cloth, etc. will be explained with reference to FIGS. 2 to 4. FIG. 3 is an explanatory diagram of a method of forming a latent image on the photosensitive pressure sensitive medium 10. As shown in the figure, first the light source 3
When light from 0 is irradiated through the original 20, only the microcapsules 11a of the photosensitive pressure sensitive medium 10 corresponding to the transparent portion 20a of the original 20 are exposed, and as a result, the microcapsules 11a in that area are hardened. As shown in the figure, when pressure is applied using the pressure roller 40, only the uncured microcapsules Ilb are destroyed, and the dye precursor inside flows out onto the color developer 4, causing color development in that part.
An identical inverse image of the image of the original 20 is formed. At this time, since the base sheet of the color developing medium of the present invention is sandblasted, the adhesion between the thermoplastic resin and the base sheet is strong and will not peel off even when passed through the pressure roller 40.
次に、第2図を用いて普通紙、布、プラスチックフィル
ム等の被画像形成体面に顕色剤画像を形成する方法を説
明する。Next, a method for forming a color developer image on the surface of an image forming object such as plain paper, cloth, plastic film, etc. will be explained using FIG.
まず、第2図で示す方法で画像の形成された顕色媒体1
の顕色剤層面4と普通紙、布、プラスチックフィルム等
の被画像形成体5とを合わせ加熱手段として加熱ローラ
6で熱圧する。すると、顕色剤層4中の顕色剤と結合剤
が溶融し、被画像形成体5に接着し、その後顕色媒体1
のベースシート2を取り除けば被画像形成体5に顕色剤
画像を転写することができる。この時熱可塑性樹脂3は
サンドブラスト加工されたベースフィルム2の表面と同
じ面状態となりつや消し状態であり傷、汚れが目立たな
い。尚、ここでは加熱手段として130℃送り速度10
mm/sの加熱ローラを用いているが、加熱可能なもの
であれば加熱ローラである必要はなくヒートプレートな
どを使用しても良い。First, a color developing medium 1 on which an image is formed by the method shown in FIG.
The color developer layer surface 4 and an image forming object 5 such as plain paper, cloth, or plastic film are brought together and hot-pressed using a heating roller 6 as a heating means. Then, the color developer and binder in the color developer layer 4 melt and adhere to the image forming object 5, and then the color developer layer 4
By removing the base sheet 2, the developer image can be transferred to the image forming body 5. At this time, the thermoplastic resin 3 is in the same surface state as the surface of the sandblasted base film 2 and is in a matte state, so that scratches and dirt are not noticeable. Here, the heating means is 130°C and a feed rate of 10
Although a heating roller of mm/s is used, it is not necessary to use a heating roller as long as it can be heated, and a heat plate or the like may be used.
次に、感光感圧媒体の組成と製造方法を簡単に説明する
。Next, the composition and manufacturing method of the photosensitive pressure sensitive medium will be briefly explained.
第3図に示す様に感光感圧媒体10は基シート12上に
マイクロカプセル11を担持したものであり、マイクロ
カプセル11は主に光硬化性樹脂。As shown in FIG. 3, the photosensitive pressure sensitive medium 10 has microcapsules 11 supported on a base sheet 12, and the microcapsules 11 are mainly made of photocurable resin.
光重合開始剤、染料前駆体を内包する。光硬化性樹脂の
代表例としてはエチレングリコールジアクリレート、エ
チレングリコールジメタクリレート。Contains photopolymerization initiator and dye precursor. Typical examples of photocurable resins are ethylene glycol diacrylate and ethylene glycol dimethacrylate.
トリメチロールプロパントリアクリレート、ジエチレン
グリコールジメタクリレートなどが、光重合開始剤とし
てはα−アルコキシフェニルケトン。Trimethylolpropane triacrylate, diethylene glycol dimethacrylate, etc. are used as a photopolymerization initiator, and α-alkoxyphenyl ketone is used as a photopolymerization initiator.
多環式キノン、ベンゾフェノン、置換ベンゾフェノン、
キサントン、チオキサントンなどが、また染料前駆体と
しては、ラクトン、ラクタム、スピロピランなどの構造
を有するもので、例えば、トリアリールメタン化合物、
ビスフェニルメタン化合物、具体的にはクリスタルバイ
オレットラクトン、ベンゾイルロイコメチレンブルーな
どが挙げられる。感光感圧媒体10のカプセル11を製
造するには、ニアセルベーション法、界面重合法等の周
知の手法にて行うことができ、このマイクロカプセル1
1内の液状物質の割合は、光硬化性樹脂を100部、染
料前駆体を3部、光重合開始剤を2.5〜4部、必要な
らば結合剤及び可塑剤をそれぞれ1部以下、そして光増
感剤を重合開始剤の10重量パーセント程度に調整する
。polycyclic quinone, benzophenone, substituted benzophenone,
Xanthone, thioxanthone, etc., and dye precursors having structures such as lactone, lactam, spiropyran, etc., such as triarylmethane compounds,
Bisphenylmethane compounds, specifically crystal violet lactone, benzoyl leucomethylene blue, and the like. The capsules 11 of the photosensitive pressure sensitive medium 10 can be manufactured by a well-known method such as near-acervation method or interfacial polymerization method.
The proportions of the liquid substances in 1 are: 100 parts of photocurable resin, 3 parts of dye precursor, 2.5 to 4 parts of photopolymerization initiator, 1 part each of binder and plasticizer if necessary, Then, the amount of photosensitizer is adjusted to about 10% by weight of the polymerization initiator.
次に本発明の顕色媒体の組成と製造法を述べる。Next, the composition and manufacturing method of the color developing medium of the present invention will be described.
顕色媒体1のベースシート2は表面の荒らされたフィル
ム、たとえば、サンドブラスト加工、エンボス加工また
は化学的エツチング加工等を施したポリエステルフィル
ム、ポリエチレンフィルム。The base sheet 2 of the color developing medium 1 is a film with a roughened surface, such as a polyester film or a polyethylene film that has been subjected to sandblasting, embossing or chemical etching.
ポリプロピレンフィルム等または金属箔が任意に使用で
きる。ベースシート2の厚みは、50〜200μm程度
が使用でき好ましくは100μm程度である。また顕色
剤層4の顕色剤としては従来の感光感圧シートに用いら
れるものは全て使用可能である。例えば酸性白土、活性
粘度、カオリン等の無機酸性物質、P−フェニルフェノ
ール等のフェノール系化合物、サリチル酸、没食子酸、
プロピルタンニン酸等の芳香族カルボン酸系化合物があ
り、単独又は複合によっても使用できる。この顕色剤に
は結合剤を任意の割合で混合することができる。更に熱
可塑性樹脂層3を構成する樹脂には、加熱により軟化ま
たは溶融し、冷却すると固化する物質を使用する。たと
えばビニルアルコール・酢酸ビニル共重合体、ポリ塩化
ビニル、塩化ビニル・酢酸ビニル共重合体等のビニル樹
脂、アクリル酸エチル、アクリル酸ブチル、シアノアク
リル酸メチル等のアクリル樹脂、スチレン樹脂、ポリア
ミド樹脂、ワックス等が挙げらられる。本実施例ではこ
の顕色媒体1のベースシート2はポリエチレンテレフタ
レートの100μmフィルムを使用した。熱可塑性樹脂
層3には、スチレン・アクリル樹脂、ポリエステルの混
合物を使用した。Polypropylene film or the like or metal foil can optionally be used. The thickness of the base sheet 2 can be about 50 to 200 μm, preferably about 100 μm. Furthermore, as the color developer for the color developer layer 4, any developer used in conventional photosensitive pressure sensitive sheets can be used. For example, acid clay, active viscosity, inorganic acid substances such as kaolin, phenolic compounds such as P-phenylphenol, salicylic acid, gallic acid,
There are aromatic carboxylic acid compounds such as propyltannic acid, which can be used alone or in combination. A binder can be mixed with this color developer in any proportion. Furthermore, the resin constituting the thermoplastic resin layer 3 is a substance that softens or melts when heated and solidifies when cooled. For example, vinyl resins such as vinyl alcohol/vinyl acetate copolymer, polyvinyl chloride, vinyl chloride/vinyl acetate copolymer, acrylic resins such as ethyl acrylate, butyl acrylate, methyl cyanoacrylate, styrene resin, polyamide resin, Examples include wax. In this example, the base sheet 2 of the color developing medium 1 was a 100 μm film of polyethylene terephthalate. For the thermoplastic resin layer 3, a mixture of styrene/acrylic resin and polyester was used.
この樹脂に選択すると、第5図に示す様に被画像形成体
5のエツジで熱可塑性樹脂層3と顕色剤層4が切断され
る。つまり切断される前では(顕色媒体1のベースシー
ト2と熱可塑性樹脂層3の接着力)〉(熱可塑性樹脂3
及び顕色剤層4のせん断に必要な応力)
(顕色媒体1の顕色剤層4と被画像形成体5の接着力)
〉(熱可塑性樹脂3及び顕色剤層4のせん断に必要な応
力)
(顕色媒体1の熱可塑性樹脂層3と顕色剤層4の接着力
)〉(熱可塑性樹脂層3及び顕色剤層4のせん断に必要
な応力)
が成立し、切断後で
(顕色媒体1の顕色剤層4と被画像形成体の接着力)〉
(顕色媒体1のベースシート2と熱可塑性樹脂層3の接
着力)
(顕色媒体1の熱可塑性樹脂層3と顕色剤層4との接着
力)〉(顕色媒体1のベースシート2と熱可塑性樹脂層
3の接着力)
が成立している。When this resin is selected, the thermoplastic resin layer 3 and the color developer layer 4 are cut at the edge of the image forming body 5 as shown in FIG. In other words, before cutting (adhesive force between base sheet 2 of color developing medium 1 and thermoplastic resin layer 3)> (thermoplastic resin 3
and the stress necessary for shearing the color developer layer 4) (Adhesive force between the color developer layer 4 of the color developer medium 1 and the image forming body 5)
〉(Stress required for shearing of thermoplastic resin 3 and color developer layer 4) (Adhesive force between thermoplastic resin layer 3 and color developer layer 4 of color developer medium 1)〉(Thermoplastic resin layer 3 and color developer layer 4) The stress required for shearing the developer layer 4) is established, and after cutting (adhesive force between the developer layer 4 of the developer medium 1 and the image forming body)
(Adhesive force between base sheet 2 of color developing medium 1 and thermoplastic resin layer 3) (Adhesive force between thermoplastic resin layer 3 and color developer layer 4 of color developing medium 1)> (Base sheet of color developing medium 1) 2 and the adhesive force between the thermoplastic resin layer 3).
また、顕色剤層4は酸性白土、ビスフェノールA、P−
フェニルフェノールを用いた。次に、塗布方法を説明す
る。熱可塑性樹脂層3として50wt%スチレンアクリ
ル共重合体エマルション(1000cps)と45wt
%のポリエステルの溶液(500c p s)を混合し
、調整後、べ−シートであるポリエチレンテレフタレー
トフィルム7テイジンマツトフイルムSM(金入(株)
)100μmに塗布し、110℃オーブンで1分間乾燥
させた。乾燥後の膜厚は10μmである。次に顕色剤層
4として、酸性白土50部、ビスフェノールA30部、
P−フェニルフェノール30部を結合剤であるポリビニ
ルアルコールの水溶液60部に分散させ、顕色剤分散溶
液とし、乾燥後の熱可塑性樹脂層3上に塗布する。塗布
後80℃のオーブンで1分間熱風乾燥させ、乾燥後15
μmの顕色剤層を得た。こうして本発明の顕色媒体は作
成される。In addition, the color developer layer 4 is made of acid clay, bisphenol A, P-
Phenylphenol was used. Next, the coating method will be explained. 50wt% styrene-acrylic copolymer emulsion (1000cps) and 45wt% as thermoplastic resin layer 3
% of polyester solution (500 cps) and after adjustment, the base sheet of polyethylene terephthalate film 7 Teijin Matsutto Film SM (Kanairi Co., Ltd.) was prepared.
) It was applied to a thickness of 100 μm and dried in an oven at 110° C. for 1 minute. The film thickness after drying is 10 μm. Next, as the color developer layer 4, 50 parts of acid clay, 30 parts of bisphenol A,
30 parts of P-phenylphenol is dispersed in 60 parts of an aqueous solution of polyvinyl alcohol as a binder to form a developer dispersion solution, which is applied onto the dried thermoplastic resin layer 3. After coating, dry with hot air in an oven at 80℃ for 1 minute, and after drying
A .mu.m color developer layer was obtained. The color developing medium of the present invention is thus created.
[発明の効果]
以上詳述したことから明らかなように、本発明によれば
、顕色媒体のベースシートが粗面とされているので、熱
可塑性樹脂とベースシートの接着力が増大し圧力定着時
にしばしば起こる熱可塑性樹脂のベースシートからの剥
離を防ぐことができる。また、普通紙、プラスチックフ
ィルム等に顕色剤画像を転写しベースシートを取り除い
た後、熱可塑性樹脂表面がマット加工したようになり傷
。[Effects of the Invention] As is clear from the detailed description above, according to the present invention, since the base sheet of the color developing medium has a rough surface, the adhesive force between the thermoplastic resin and the base sheet increases and pressure is reduced. It is possible to prevent the thermoplastic resin from peeling off from the base sheet, which often occurs during fixing. Also, after transferring the developer image to plain paper, plastic film, etc. and removing the base sheet, the thermoplastic resin surface becomes matte and scratches.
汚れが目立たなくなり見栄えもよくなる。Dirt becomes less noticeable and the appearance improves.
第1図から第5図までは本発明を具体化した実施例を示
すもので、第1図は顕色媒体の断面図、第2図は被画像
形成体面に顕色剤画像を形成する方法の説明図、第3図
は感光感圧媒体に潜像を形成する方法の説明図、第4図
は顕色媒体に可視像を形成する方法の説明図、第5図は
熱可塑性樹脂の膜性と接着性の関係を示す図である。
図中、1は顕色媒体、2はベースシート、3は熱可塑性
樹脂層、4は顕色剤層である。1 to 5 show embodiments embodying the present invention. FIG. 1 is a cross-sectional view of a color developing medium, and FIG. 2 is a method for forming a color developer image on the surface of an image-forming object. FIG. 3 is an explanatory diagram of a method for forming a latent image on a photosensitive pressure-sensitive medium. FIG. 4 is an explanatory diagram of a method for forming a visible image on a color developing medium. FIG. 3 is a diagram showing the relationship between film properties and adhesive properties. In the figure, 1 is a color developing medium, 2 is a base sheet, 3 is a thermoplastic resin layer, and 4 is a color developer layer.
Claims (1)
樹脂層上に少なくとも染料前駆体と反応してこれを発色
させる顕色剤層を有する顕色媒体において、 前記ベースシートの両面または片面を粗面としたことを
特徴とする顕色媒体。 2、前記ベースシートの両面または片面がサンドブラス
ト加工を施されたフィルムである請求項1に記載の顕色
媒体。 3、前記ベースシートの両面または片面がエンボス加工
を施されたフィルムである請求項1に記載の顕色媒体。 4、前記ベースシートの両面または片面が、化学的エッ
チング加工を施されたフィルムである請求項1に記載の
顕色媒体。[Scope of Claims] 1. A color developing medium having a thermoplastic resin layer on a base sheet, and further a color developer layer on the thermoplastic resin layer that reacts with at least a dye precursor to develop color therein, comprising: A color developing medium characterized by having a rough surface on both or one side. 2. The color developing medium according to claim 1, wherein both or one side of the base sheet is a film that has been sandblasted. 3. The color developing medium according to claim 1, wherein the base sheet is a film that is embossed on both or one side. 4. The color developing medium according to claim 1, wherein both or one side of the base sheet is a film subjected to chemical etching processing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1217819A JPH0381185A (en) | 1989-08-24 | 1989-08-24 | Coupling medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1217819A JPH0381185A (en) | 1989-08-24 | 1989-08-24 | Coupling medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0381185A true JPH0381185A (en) | 1991-04-05 |
Family
ID=16710241
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1217819A Pending JPH0381185A (en) | 1989-08-24 | 1989-08-24 | Coupling medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0381185A (en) |
-
1989
- 1989-08-24 JP JP1217819A patent/JPH0381185A/en active Pending
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